Stellate cells in livers of dogs with portal vein hypoperfusion

Abstract

Hepatic stellate cells play a crucial role in the development of liver fibrosis. In a damaged liver, stellate cells undergo activation, which is manifested as a change of their phenotype: differentiation of stellate cells to myofibroblast-type cells, expression of alpha-Smooth Muscle Actin, their proliferation and a reduction in the size of cytoplasmic lipid droplets. The aim of this study was to determine the number and morphology of stellate cells in the canine liver affected by congenital portosystemic shunt (PSS) and portal vein hypoplasia – hepatic microvascular dysplasia (PVH-HMD). The material for investigation were archived paraffin blocks with liver samples collected supravitally from six dogs with PSS, six dogs with PVH-HMD and six healthy dogs. On the HE-stained sections, the number of stellate cells per 100 hepatocytes was counted (Sztark method) and the diameter of veins in the hepatic triads was measured (light microscope Olympus BX 43, SC30 camera, CellSens Entry 2011 Olympus). In addition, the diameter of lipid droplets in stellate cells was measured (computed image analysis system LUCIA 4.21). The results were analysed statistically (the Kruskal-Wallis test followed by Dunn’s post-hoc procedure; significance level (α) at 0.05; Statistica 12 StatSoft Inc.). The degree of liver fibrosis was determined (Masson’s method of slide stain; Scheuer scale). The liver samples from the dogs with PSS and PVH-HMD were stained immunohistochemically with Monoclonal Mouse Anti-Human Smooth Muscle Actin (α-SMA), clone 1A4, antibodies (DAKO). Portosystemic shunt and primary portal vein hypoplasia in the dog results in a reduction in the diameter of portal vein branches and in insufficient portal blood flow through the liver. In the material investigated, this was particularly evident in the animals affected by PSS: such dogs had a significantly smaller diameter of the veins than did the healthy dogs (p<0.001) or the dogs with PVH-HMD (p=0.023). Fibrosis and the expression of α-SMA were stronger in the dogs with PSS than in those with PVH-HMD. Moreover, the dogs with PSS had a significantly higher average number of stellate cells than the healthy animals (p=0.007) did. However, the examination of the material revealed an enlargement of cytoplasmic lipid droplets: the dogs with PSS had a significantly larger diameter of lipid vacuoles in the cytoplasm of stellate cells than did the healthy animals (p<0.001) or the dogs with PVH-HMD (p=0.043); the dogs with PVH-HMD had lipid droplets with a significantly larger diameter than the healthy animals (p<0.001) did. Hypoperfusion of the liver and the accompanying regressive lesions in hepatocytes result mainly in an increased number of stellate cells and stronger expression of α-SMA, while cytoplasmic lipid droplets in the stellate cells are not reduced in size. The present study indicates the need for detailed analyses of clinical cases and warrants further comprehensive studies of comparative hepatopathology because it demonstrates differences between humans and dogs in the morphological indicators of hepatic stellate cell activation in chronic liver damage.

Retrospective liver histomorphological analysis in dogs in instances of clinical suspicion of congenital portosystemic shunt

“…Even if the cross-section of the vein was smaller in diameter than in the liver of the healthy dog, it was generally visible. In our previous investigations we determined that in animals with microvascular dysplasia the median diameter of the veins in the portal areas was 36.9 μm, whereas in dogs with congenital portosystemic shunts it was 19.1 μm (significantly smaller), and in healthy dogs was 82.1 μm (16). Moreover, fibrosis was more pronounced in dogs with portosystemic shunts compared to dogs with microvascular dysplasia.…”

Polish Journal of Veterinary Sciences

“…However, cPSS is well-known to lead to dramatic local circulatory disturbances. In many patients the portal venous system is hypoplastic (Sobczak-Filipiak et al 2018a, and the blood pressure changes in these veins, and even reversed direction of blood flow (hepatofugal instead of hepatopetal) are not uncommon (Morandi et al 2010). As the portal vein collects branches from the pancreas, circulatory abnormalities could be potentially responsible for the abnormal pancreatic structure.…”

Polish Journal of Veterinary Sciences

“…However, cPSS is well-known to lead to dramatic local circulatory disturbances. In many patients the portal venous system is hypoplastic (Sobczak-Filipiak et al 2018a, and the blood pressure changes in these veins, and even reversed direction of blood flow (hepatofugal instead of hepatopetal) are not uncommon (Morandi et al 2010). As the portal vein collects branches from the pancreas, circulatory abnormalities could be potentially responsible for the abnormal pancreatic structure.…”